Canonical Allele Identifier: CA363310319
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355372T>G , CM000668.2:g.31355372T>G GRCh38
NC_000006.11:g.31323149T>G , CM000668.1:g.31323149T>G GRCh37
NC_000006.10:g.31431128T>G NCBI36
NG_023187.1:g.6841A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.2887A>C
ENST00000481849.6:n.2313A>C
ENST00000497377.6:n.2313A>C
ENST00000640094.2:c.840A>C ENSP00000491275.2:p.Arg280Ser
ENST00000696558.1:c.909A>C ENSP00000512716.1:n.909A>C
ENST00000696559.1:c.840A>C ENSP00000512717.1:p.Arg280Ser
ENST00000696560.1:c.840A>C ENSP00000512718.1:p.Arg280Ser
ENST00000696561.1:c.840A>C ENSP00000512719.1:p.Arg280Ser
ENST00000696562.1:c.840A>C ENSP00000512720.1:p.Arg280Ser
ENST00000412585.7:c.840A>C MANE Select ENSP00000399168.2:p.Arg280Ser
ENST00000640094.1:c.33A>C ENSP00000491275.1:p.Arg11Ser
ENST00000412585.6:c.840A>C ENSP00000399168.2:p.Arg280Ser
ENST00000463574.1:n.431A>C
NM_005514.6:c.840A>C NP_005505.2:p.Arg280Ser
XM_011514556.1:c.873A>C XP_011512858.1:p.Arg291Ser
XM_011514557.1:c.840A>C XP_011512859.1:p.Arg280Ser
XR_926175.1:n.1279A>C
NM_005514.7:c.840A>C NP_005505.2:p.Arg280Ser
NM_005514.8:c.840A>C MANE Select NP_005505.2:p.Arg280Ser